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1 August 2002 Developmental Capacity and Chromosome Number in the Offspring of Artificially Produced Autotetraploids of Rana nigromaculata
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Abstract

A large number of autotetraploids of Rana nigromaculata were produced in order to assess their developmental capacity and chromosome number in their offspring. An original autotetraploid male was first produced by transplanting a nucleus from an embryo (triploid) into an unfertilized egg. Next, eggs were inseminated with sperm of the autotetraploid male, then cold-treated to obtain first-, second-, and third-generation offspring. According to an investigation of the chromosome numbers of the tadpoles by the tail-tip squash method, the three generations of offspring included many tetraploids (50–80%), as well as some diploids, triploids, hexaploids and mosaics at the early tadpole stage. In addition, several percent of the second- and third-generation offspring were found to be aneuploids. Evidently, a complete set of diploid chromosomes was not precisely transferred to all of the next-generation offspring from the sperm of the artificially produced autotetraploid males. These observations suggest that there were some abnormalities in the course of spermatogenesis in the male autotetraploid frogs.

INTRODUCTION

It has proven to be very difficult to artificially produce mature tetraploid amphibians, in spite of exhaustive efforts taken by investigators from as far back as the 1940's. While it has been possible to obtain embryos of polyploid amphibians for quite some time, difficulties in nurturing tadpoles or juvenile animals in the laboratory thwarted all attempts to rear amphibians to full adulthood until 1949.

Humphrey and Fankhauser (1949) were the first to produce mature autotetraploid amphibians in their experiments using Ambystoma mexicanum. Thereafter, mature autotetraploids were obtained in Xenopus laevis by Gurdon (1959), in Rana japonica by Kawamura et al. (1960, 1963b), and in Pleurodeles wartl by Beetschen (1962, 1967). In each of these cases, only a very small number of tetraploid amphibians was obtained. In the most recent experiments, Kawamura and Nishioka (1960, 1963a) and Nishioka and Okumoto (1983) obtained fairly fertile allotetraploids (amphidiploids) between R. porosa brevipoda and R. nigromaculata, and between R. nigromaculata and R. plancyi chosenica. Kawamura et al. (1983) produced autotetraploids of R. porosa brevipoda and R. nigromaculata by mating autotriploid females with diploid males. The former autotetraploids died after metamorphosis, but the latter were reared to three males (0.1% of treated eggs) that survived to sexual maturity. Mating with these males was not attempted.

In the present study, the author attempted to produce autotetraploids of R. nigromaculata, examine their fertility, and establish a procedure for producing and maintaining the autotetraploidy through several generations. Moreover, he investigated the chromosome numbers of the offspring produced from fertilized eggs with autotetraploid males.

MATERIALS AND METHODS

Males and females of the Japanese pond frog R. nigromaculata Hallowell (2n=26) were collected from Hiro, Kure City, Hiroshima Prefecture. The following procedures were carried out to produce autotetraploid frogs (Fig. 1).

  1. Production of an original autotetraploid male

    Ovulation was stimulated by cutaneous implantation of pituitary glands. Sperm suspension was prepared by anesthetizing and sacrificing a field-caught male and macerating its testes in dechlorinated tap water. Artificially inseminated eggs were refrigerated for 2.5 hr at 2°C to suppress the extrusion of their second polar bodies and make triploid embryos (Fankhauser and Griffiths, 1939; Nishioka, 1972). When these embryos developed into the late blastula stage, a single sub-surface cell nucleus from the blastula embryo was transplanted into each unfertilized egg (Briggs and King, 1952; Kondo, 1978). These transplanted eggs were then reared carefully and were bred to the later stage. At the early tadpole stage, the number of chromosomes was examined by the squash method after water-pretreatment of the tail-tips (Makino and Nishimura, 1952). Only one tadpole grew up to become a mature male frog.

  2. Production of the first-, second-, and third-generation offspring of autotetraploid R. nigromaculata

    To obtain the first-generation autotetraploids, eggs from a field-caught female were inseminated with the sperm from an anesthetized autotetraploid male, and then refrigerated to suppress the extrusion of their second polar bodies. Only tadpoles confirmed to be tetraploidy were reared until maturation.

    The second-generation offspring were produced by mating seven field-caught females with seven autotetraploid males of the first-generation offspring, and the third-generation offspring were produced by mating nine females of diploid control offspring with five autotetraploid males of the second-generation offspring.

    The tadpoles were fed on boiled spinach outdoors until metamorphosis, then the metamorphosed frogs were fed on crickets in a room.

    In this paper, the acronyms NN, NNN, and NNNN are used to denote autodiploids, autotriploids, and autotetraploids of R. nigromaculata, respectively.

Fig. 1

Diagrams illustrating methods for producing offspring of normal control diploids (A) and the first-, second- and third-generation offspring of autotetraploids (B) in R. nigromaculata. See the text in details.

i0289-0003-19-8-877-f01.tif

RESULTS

  1. An autotetraploid male parent

    Several brothers from blastulae whose nuclei had been transplanted into unfertilized eggs were bred until the early tadpole stage, then their tail-tips were squashed to examine the ploidy and number of chromosomes. As expected, they were triploids possessing three genome sets consisting of five large and eight small chromosomes (Nishioka, 1972). This strongly suggested that the transplanted nucleus was also triploidy. Moreover, according to the chromosome count, a tadpole produced by nuclear transplantation was exactly tetraploid, having four genome sets consisting of five large and eight small chromosomes. This tadpole attained sexual maturity and grow to become a healthy male with a body length of 65mm.

  2. The first-generation offspring

    A total of 552 eggs from one field-caught female were fertilized with the sperm of testes taken from the abovementioned autotetraploid male in an anesthetized condition, and then refrigerated shortly after insemination. The developmental capacity of the first-generation offspring is presented in Table 1. In an analysis of the ploidy of 29 normally feeding tadpoles, 24 (82.8%) tadpoles were tetraploids, one was diploid, two were triploids, and the remaining two were diplo-tetraploid and triplo-pentaploid mosaics (Table 2). Eighteen of 24 tetraploid tadpoles completed metamorphosis and attained sexual maturity. There were nine females and nine males. Among the control diploid, autotriploid, and autotetraploid frogs of each sex, there were no differences in body sizes (64–67mm) or color pattern (Fig. 2).

Table 1

Developmental capacity of the 1st-generation offspring produced from the eggs refrigerated shortly after insemination with sperm of an autotetraploid male and the controls

i0289-0003-19-8-877-t01.gif

Table 2

Ploidy of feeding tadpoles of the 1st-generation offspring and the controls

i0289-0003-19-8-877-t02.gif

Fig. 2

Mature control diploid (A, D), control autotriploid (B, E) and the first-generation autotetraploid R. nigromaculata (C, F). A, B and C are females and D, E and F are males. There was no difference among diploid, autotriploid and autotetraploid frogs in appearance. Scale bar represents 1cm.

i0289-0003-19-8-877-f02.tif

(3) The second-generation offspring

A total of 6,064 eggs from seven field-caught females were fertilized with the sperm of seven autotetraploid males of the first-generation offspring and then refrigerated shortly after insemination. Table 3 shows the developmental capacity of the second generation. In total, 379 (6.3%) embryos developed into normally feeding tadpoles.

Table 3

Developmental capacity of the 2nd-generation offspring produced from the eggs refrigerated shortly after insemination with sperm of autotetraploid males and the controls

i0289-0003-19-8-877-t03.gif

According to a chromosomal analysis on 364 of 379 normal tadpoles, 272 (74.7%) tadpoles were tetraploids, 30 (8.2%) were diploids, two (0.5%) were triploids, three (0.8%) were hexaploids, nine (2.5%) were aneuploids, and the remaining 48 (13.2%) were mosaics. The nine aneuploids consisted of five hypotetraploids [including two (4n-3), one (4n-2), and two (4n-1)] and four hypertetraploids [including two (4n+1), one (4n+2) and one (4n+3)]. The other 48 tad-poles consisted of one (2n+4n), 41 (2n+6n), and six (3n+5n) mosaics (Table 4, Fig. 3).

Table 4

Number of chromosomes of feeding tadpoles of the 2nd-generation offspring and the controls

i0289-0003-19-8-877-t04.gif

Fig. 3

Karyotypes of a control diploid (A), an autotetraploid (B), and an aneuploid (C) of the second-generation offspring observed by the tail-tip squash method. Karyotype of the autotetraploid (B) possessed four genome sets consisting of five large (Nos. 1–5) and eight small chromosomes (Nos. 6–13). One of chromosome No. 8 and two of chromosome No. 11 were lost in the karyotype of the hypotetraploid (4n-3) (C). Scale bar represents 10 μm.

i0289-0003-19-8-877-f03.tif

Of the 272 tetraploid tadpoles, 241 (88.6%) completed metamorphosis and 122 (44.9%) attained sexual maturity. Of a total 202 juvenile and mature frogs analyzed, 152 (75.2%) were females and 50 (24.8%) were males.

(4) The third-generation offspring

The nine females used for the production of the third-generation offspring were derived from the diploid control offspring of the first generation. Of these nine females, five (Nos. 1–5) were mated with three autotetraploid males (Nos. 1–3) derived from the male No. 2 used to produce the second generation, and the other four females (Nos. 6–9) were mated with two autotetraploid males (Nos. 4 and 5) derived from the male No. 5 used to obtain the second generation. A total of 9,132 eggs were fertilized with the sperm of autotetraploid males and refrigerated shortly after insemination to block the extrusion of their second polar bodies. Table 5 shows the developmental capacity of the third generation. In total, 1,708 (18.7%) embryos developed into normally feeding tadpoles.

Table 5

Developmental capacity of the 3rd generation offspring produced from the eggs refrigerated shortly after insemination with sperm of autotetraploid males and the controls

i0289-0003-19-8-877-t05.gif

A chromosomal examination of 1,128 of the 1,708 normal tadpoles revealed 590 (52.3%) tetraploids, 84 (7.4%) diploids, 257 (22.8%) triploids, one (0.1%) pentaploid, and three (0.3%) hexaploids. The remaining 193 tadpoles were 42 (3.7%) aneuploids and 151 (13.4%) mosaics. The 42 aneuploids consisted of five (0.4%) hyperdiploids [including three (2n+1) and two (2n+2)], nine (0.8%) hypotriploids [including five (3n-2) and four (3n-1)], six (0.5%) hypertriploids [including three (3n+1), one (3n+1), and two (3n+3)], 10 (0.9%) hypotetraploids [including two (4n-3), two (4n-2), and six (4n-1)], and 12 (1.1%) hypertetraploids [including six (4n+1), five (4n+2), and one (4n+3)]. The remaining 151 individuals consisted of 44 (2n+4n), 92 (2n+6n), six (3n+5n), and nine (3n+4n, 2n+3n+4n+5n, and others) mosaics (Table 6).

Table 6

Number of chromosomes of feeding tadpoles of the 3rd-generation offspring and the contro

i0289-0003-19-8-877-t06.gif

Of the 590 tetraploid tadpoles, 575 (97.5%) completed metamorphosis and 466 (79.0%) of the frogs attained sexual maturity. Of a total 511 of analyzed juvenile and mature frogs, there were 328 (64.2%) females and 183 (35.8%) males.

DISCUSSION

The present results on R. nigromaculata show that this species was able to produce next-generation autotetraploids from more than half of the total eggs used by consecutive procedures of nuclear transplantation of a triploid nucleus, fertilization with diploid sperm, and egg refrigeration. Numerous descendants with the same viability as the control diploids were obtained through three generations. On the other hand, a small number of mosaics and aneuploid tadpoles were also produced through the three generations. If the aneuploids were the product of abnormal processes of meiosis in testis, it may be valuable to examine the pairing of meiotic chromosomes in the first reduction division of spermatogenesis of autotetraploid males. The autotetraploid male used for the present study developed from an egg transplanted with a triploid blastula nucleus taken from a sibling fertilized egg. That is to say, the original autotetraploid possessed three genome sets from the same mother and one genome set from a father. Fankhauser and Humphrey (1950) produced autotetraploids of Ambystoma mexicanum by matings between triploid females and diploid males. Kawamura and Nishioka (1960) obtained autotetraploids of R. japonica by two methods, i.e., nuclear transplantation of a diploid blastula nucleus into diploid fertilized eggs, or heat-shock treatment of the diploid fertilized eggs before the first cleavages. If such methods can be applied to produce autotetraploids of R. nigromaculata, it is interesting to analyze the chromosome numbers of the offspring of autotetraploids to compare the incidence of the aneuploids among tetraploid tadpoles produced by different methods.

Autotetraploid males from the species A. mexicanum (Humphrey and Fankhauser, 1956; Fankhauser and Humphrey, 1959) and X. laevis (Gurdon, 1959) were completely sterile. Among tetraploid silkworms obtained by Vereiskaya and Astaurov (1962), amphidiploid females derived from matings between Bombyx mori and B. mandarina were as fertile as autotetraploid females of B. mori, while amphidiploid males from the same parentage were partly fertile, and autotetraploid males were completely sterile. In the plant kingdom, a number of artificially synthesized tetraploid plants have been reported (Myers, 1940; Lamm, 1943). A true autopolyploid is usually sterile because of improper pairing of the chromosomes at meiosis (Bell, 1967); the gametogenesis in autotetraploid plants is generally abnormal. The above findings are remarkably different from the findings on the fertility of autotetraploids from the species R. nigromaculata or R. japonica. However, it may be possible to produce fertile autotetraploid males of the species urodeles or Xenopus artificially in the future.

Fertile autotetraploid males are very useful materials for producing autotetraploids, amphidiploids, androgenetic homospermic diploids, and diploid nucleo-cytoplasmic hybrids in amphibians (Kawamura and Nishioka, 1963b).

When the same methods are applied to lower vertebrates, these artificial polyploids and diploids will be useful for the improvement of breeds in many species. Moreover, the artificial polyploid and diploid animals may help clarify the process of the polyploid species formation found in some areas of the world.

Acknowledgments

The author wishes to express his sincere thanks to Emeritus Professor Toshijiro Kawamura and Emeritus Professor Midori Nishioka of Hiroshima University for their kind guidance throughout the course of this study, and also to Professor Katsutoshi Yoshizato, Professor Yoshio Yaoita, and Professor Masayuki Sumida of Hiroshima University for their encouragement and critical reviews of the manuscript.

REFERENCES

1.

J-C. Beetschen 1962. Sur la descendance de femelles tetraploides croisees avec des males diploides, chez l'amphibien urodele, Pleurodeles waltlii. C R Acad Sci (Paris) 255:3068–3070. Google Scholar

2.

J-C. Beetschen 1967. Cinq generations d'individus polyploides chez le triton Pleurodeles waltlii Michah. C R Soc Biol (Paris) 161:930–936. Google Scholar

3.

C. R. Bell 1967. Plant Variation and Classification. Wadsworth Publ Co. Belmont, California. Google Scholar

4.

R. Briggs and T. J. King . 1952. Transplantation of living nuclei from blastula cells into enucleated frogs' eggs. Proc Natl Acad Sci USA 38:455–463. Google Scholar

5.

G. Fankhauser and R. B. Griffiths . 1939. Induction of triploidy and haploidy in the newt, Triturus viridescens, by cold treatment of unsegmented eggs. Proc Nat Acad Sci USA 25:233–238. Google Scholar

6.

G. Fankhauser and R. R. Humphrey . 1950. Chromosome number and development of progeny of triploid axolotl females mated with diploid males. J Exp Zool 115:207–249. Google Scholar

7.

G. Fankhauser and R. R. Humphrey . 1959. The origin of spontaneous heteroploids in the progeny of diploid, triploid, and tetraploid axolotl females. J Exp Zool 142:379–422. Google Scholar

8.

J. B. Gurdon 1959. Tetraploid frogs. J Exp Zool 141:519–544. Google Scholar

9.

R. R. Humphrey and G. Fankhauser . 1949. Three generations of polyploids in ambystomid salamanders. J Hered 40:7–14. Google Scholar

10.

R. R. Humphrey and G. Fankhauser . 1956. Structure and functional capacity of the ovaries of higher polyploids (4N, 5N) in the Mexican axolotl (Siredon or Ambystoma mexicanum). J Morphol 98:161–198. Google Scholar

11.

T. Kawamura and M. Nishioka . 1960. Amphidiploid frogs produced by artificial means. J Sci Hiroshima Univ Ser B Div 1 18:195–220. Google Scholar

12.

T. Kawamura and M. Nishioka . 1963a. Reproductive capacity of amphidiploid male produced by nuclear transplantation in Amphibian. J Sci Hiroshima Univ Ser B Div 1 21:1–13. Google Scholar

13.

T. Kawamura and M. Nishioka . 1963b. Autotetraploids and the production of allopentaploids and diploid nucleo-cytoplasmic hybrids in pond frogs. J Sci Hiroshima Univ Ser B Div 1 21:85–106. Google Scholar

14.

T. Kawamura, M. Nishioka, and Y. Myorei . 1960. On reproductive ability of autotetraploid brown frogs, Rana japonica. Jpn J Genet 35:273–274. In Japanese. Google Scholar

15.

T. Kawamura, M. Nishioka, and Y. Myorei . 1963. Reproductive capacity of autotetraploid males in brown frogs. J Sci Hiroshima Univ Ser B Div 1 21:15–24. Google Scholar

16.

T. Kawamura, M. Nishioka, and H. Okumoto . 1983. Production of auto-tetraploids and amphidiploids from auto- and allotriploids in Rana nigromaculata and Rana brevipoda. Sci Rep Lab Amphibian Biol Hiroshima Univ 6:47–80. Google Scholar

17.

Y. Kondo 1978. Behavior of foreign nucleus transplanted into a Rana nigromaculata egg. Zool Mag 87:207–215. In Japanese with English abstract. Google Scholar

18.

R. Lamm 1943. Notes on an octaploid Solanum punae plant. Hereditas 29:193–195. Google Scholar

19.

S. Makino and I. Nishimura . 1952. Water-pretreatment squash technic: A new and simple practical method for the chromosome study of animals. Stain Tech 27:1–7. Google Scholar

20.

W. M. Myers 1940. Tetrasomic inheritance in Dactylis glomerata. Genetics 25:126. Google Scholar

21.

M. Nishioka 1972. The karyotypes of two sibling species of Japanese pond frogs, with special reference to those the diploid and triploid hybrids. Sci Rep Lab Amphibian Biol Hiroshima Univ 1:319–337. Google Scholar

22.

M. Nishioka and H. Okumoto . 1983. Reproductive capacity and progeny of amphidiploids between Rana nigromaculata and Rana plancyi chosenica. Sci Rep Lab Amphibian Biol Hiroshima Univ 6:141–181. Google Scholar

23.

V. N. Vereiskaya and B. L. Astaurov . 1962. Experimental proof concerning the possibility to overcome male sterility in tetraploid silkworms by means of amphidiploidy (2n Bombyx mori + 2n B. mandarina). Byull Mosk Obshch Isp Prir Otd Biol 67:45–55. Google Scholar
Yasuyuki Kondo "Developmental Capacity and Chromosome Number in the Offspring of Artificially Produced Autotetraploids of Rana nigromaculata," Zoological Science 19(8), 877-883, (1 August 2002). https://doi.org/10.2108/zsj.19.877
Received: 21 January 2002; Accepted: 1 June 2002; Published: 1 August 2002
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